Automated pediatric defibrillator

ABSTRACT

A device for assisting a rescuer in delivering therapy to an adult or pediatric patient, the device including a user interface comprising a display and/or audio speakers, the user interface being configured to deliver prompts to a rescuer to assist the rescuer in delivering therapy to a patient; a processor configured to provide prompts to the user interface and to perform an ECG analysis algorithm on ECG information detected from the patient; at least one detection element configured to determine without rescuer input via the user interface that a pediatric patient is being treated; wherein, if a pediatric patient is detected, the processor modifies the ECG analysis algorithm or the prompts provided to the user interface to use an ECG analysis algorithm or prompts adapted for a pediatric patient rather than for an adult patient.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No.60/561,493, filed on Apr. 12, 2004.

TECHNICAL FIELD

This invention relates to the treatment of cardiac arrest in pediatricpopulations with automatic external defibrillators (AEDs).

BACKGROUND

Automatic External Defibrillators (AEDs) are used by non-medicalpersonnel to defibrillate victims of cardiac arrest the prevalence ofwhich is approximately 600,000 people per year, worldwide. In the past,these AEDs had only been available for the adult population, and thepediatric arrest victims were forced to wait valuable minutes for theprofessional rescuers such as paramedics, doctors or nurses to arrive.AEDs are now available that are designed specifically to be compatiblefor use on children. Because defibrillation energies are lower withchildren, various methods have been developed to accommodate this factand provide a means of switching defibrillation energies if a pediatricarrest victim is present. One method, described in U.S. Pat. No.6,101,413, determines a pediatric arrest victim is present if the AEDdetects that electrodes specifically designed for use with children areattached to the device, in which case the energy levels and voiceprompts associated with energy delivery are adjusted to conform withthose most appropriate for children. U.S. patent application No.2003/0195567A1 describes a method that determines a victim is a childbased on user input form the AED operator. The energy levels are setbased on such indirect means as a measurement of the patient, e.g., thelength of an anatomical feature of the victim may be correlated withinthe AED to a specific energy level.

Resuscitation treatments for patients suffering from cardiac arrestgenerally include clearing and opening the patient's airway, providingrescue breathing for the patient, and applying chest compressions toprovide blood flow to the victim's heart, brain and other vital organs.If the patient has a shockable heart rhythm, resuscitation also mayinclude defibrillation therapy. The term basic life support (BLS)involves all the following elements: initial assessment; airwaymaintenance; expired air ventilation (rescue breathing); and chestcompression. When all three [airway breathing, and circulation,including chest compressions] are combined, the term cardiopulmonaryresuscitation (CPR) is used. In the case of pediatric arrest, CPR takeson a heightened prominence based on the fact that cardiac arrest is rarein children, and many more children are affected by respiratory arrestdue to choking, drowning, poisoning and asthma.

There are many different kinds of abnormal heart rhythms, some of whichcan be treated by defibrillation therapy (“shockable rhythms”) and somewhich cannot (non-shockable rhythms”). For example, most ECG rhythmsthat produce significant cardiac output are considered non-shockable(examples include normal sinus rhythms, certain bradycardias, and sinustachycardias). There are also several abnormal ECG rhythms that do notresult in significant cardiac output but are still considerednon-shockable, since defibrillation treatment is usually ineffectiveunder these conditions. Examples of these non-shockable rhythms includeasystole, electromechanical disassociation and other pulselesselectrical activity. Although a patient cannot remain alive with thesenon-viable, non-shockable rhythms, applying shocks will not help convertthe rhythm. The primary examples of shockable rhythms, for which thecaregiver should perform defibrillation, include ventricularfibrillation, ventricular tachycardia, and ventricular flutter.

The current protocols recommended by the American Heart Association(AHA) are as follows: after using a defibrillator to apply one or moreshocks to a patient who has a shockable ECG rhythm, the patient maynevertheless remain unconscious, in a shockable or non-shockable,perfusing or non-perfusing rhythm. If a non-perfusing rhythm is present,the caregiver may then resort to performing CPR for a period of time inorder to provide continuing blood flow and oxygen to the patient'sheart, brain and other vital organs. If a shockable rhythm continues toexist or develops during the delivery of CPR, further defibrillationattempts may be undertaken following this period of cardiopulmonaryresuscitation. As long as the patient remains unconscious and withouteffective circulation, the caregiver can alternate between use of thedefibrillator (for analyzing the electrical rhythm and possibly applyinga shock) and performing cardio-pulmonary resuscitation (CPR). CPRgenerally involves a repeating pattern of five or fifteen chestcompressions followed by a pause during which two rescue breaths aregiven.

Defibrillation can be performed using an AED. The American HeartAssociation, European Resuscitation Council, and other similar agenciesprovide protocols for the treatment of victims of cardiac arrest thatinclude the use of AEDs. These protocols define a sequence of steps tobe followed in accessing the victim's condition and determining theappropriate treatments to be delivered during resuscitation. Caregiverswho may be required to use an AED are trained to follow these protocols.

Most automatic external defibrillators are actually semi-automaticexternal defibrillators (SAEDs), which require the caregiver to press astart or analyze button, after which the defibrillator analyzes thepatient's ECG rhythm and advises the caregiver to provide a shock to thepatient if the electrical rhythm is shockable. The caregiver is thenresponsible for pressing a control button to deliver the shock.Following shock delivery, the SAED may reanalyze the patient's ECGrhythm, automatically or manually, and advise additional shocks orinstruct the caregiver to check the patient for signs of circulation(indicating that the defibrillation treatment was successful or that therhythm is non-shockable) and to begin CPR if circulation has not beenrestored by the defibrillation attempts. Fully automatic externaldefibrillators, on the other hand, do not wait for user interventionbefore applying defibrillation shocks. As used below, automatic externaldefibrillators (AEDs) include semi-automatic external defibrillators(SAEDs).

Automated External Defibrillators include signal processing softwarethat analyzes ECG signals acquired from the victim to determine when acardiac arrhythmia such as Ventricular Fibrillation (VF) or shockableventricular tachycardia (VT) exists. Usually, these algorithms aredesigned to perform ECG analyses at specific times during the rescueevent. The first ECG analysis is usually initiated within a few secondsfollowing attachment of the defibrillation electrodes to the patient.Subsequent ECG analyses may or may not be initiated based upon theresults of the first analysis. Typically if the first analysis detects ashockable rhythm, the rescuer is advised to deliver a defibrillationshock. Following the shock delivery a second analysis is automaticallyinitiated to determine whether the defibrillation treatment wassuccessful or not (i.e. the shockable ECG rhythm has been converted to anormal or other non-shockable rhythm). If this second analysis detectsthe continuing presence of a shockable arrhythmia, the AED advises theuser to deliver a second defibrillation treatment. A third ECG analysismay then be initiated to determine whether the second shock was or wasnot effective. If a shockable rhythm persists, the rescuer is thenadvised to deliver a third defibrillation treatment.

The typical algorithms process the ECG for measured features which willdifferentiate the rhythm as shockable (ventricular fibrillation (VF) andventricular tachycardia (VT)) or non-shockable rhythms (normal sinusrhythms (NSR), abnormal rhythms (ABN), non-shockable VT's and asystole).Some of these features include R to R interval averaging, R to Rinterval variance, average and maximum signal amplitude, measures ofbaseline isoelectric time, QRS width, ECG first differencedistributions, and parameters from frequency domain analysis¹ Analysesof annotated ECG databases establish the distribution of values for agiven feature for shockable and non-shockable rhythms. Appropriatedecision logic techniques can be used to combine this knowledge andproduce the shock or non-shock decision.

Although AEDs have been designed for use on adults and the ECGarrhythmia logic has been developed for the adult population, there is aclear need to extend the use of AEDs to children with cardiac arrest.Recent literature have reported the accuracies of adult based AEDarrhythmia algorithms on ECG databases collected from children and haveconcluded they are safe and effective. However, there are significantdifferences between adult and pediatric ECG rhythms. For example, thepediatric ECG exhibits faster normal heart rates, narrower QRS widths,and shorter PR and QT intervals as compared to adults. Shockableventricular tachycardia occurs at much higher rates (>200 BPM) inpediatric subjects than adults (>150 BPM).

Following the third defibrillator shock or when any of the analysesdescribed above detects a non-shockable rhythm, treatment protocolsrecommended by the American Heart Association and European ResuscitationCouncil require the rescuer to check the patient's pulse or to evaluatethe patient for signs of circulation. If no pulse or signs ofcirculation are present, the rescuer is trained to perform CPR on thevictim for a period of one or more minutes. Following this period ofcardiopulmonary resuscitation (that includes rescue breathing and chestcompressions) the AED reinitiates a series of up to three additional ECGanalyses interspersed with appropriate defibrillation treatments asdescribed above. The sequence of 3 ECG analyses/defibrillation shocksfollowed by 1-3 minutes of CPR, continues in a repetitive fashion for aslong as the AED's power is turned on and the patient is connected to theAED device. Typically, the AED provides audio prompts to inform therescuer when analyses are about to begin, what the analysis results wereand when to start and stop the delivery of CPR.

The AED can be used on adult and pediatric patients. However, theAmerican Heart Association recommends a different protocol in the rescueof pediatric victims compared to the adult rescue protocol particularlywith regards to the application of CPR. Because of the heightenedprominence of airway and breathing with pediatric arrest victims, theAHA recommends that prior even to calling and activating emergencymedical services (EMS) system, the child's airway is first checked forobstructions, the airway is cleared, and mouth to mouth breathing isperformed in order to provide what is usually the primary treatment ofrespiration to the child. The AHA recommends a ratio 15 chestcompressions to two ventilations in the case of an adult victim and aratio of five chest compressions to one ventilation in the case ofpediatric victims. The recommended rate of compressions in both adultand pediatric victims is 100 compressions per minute. The rationale forthis difference in compression to ventilation ratios is that: 1) themost common cause in pediatric (<8 years of age) arrest is respiratory;and 2) respiratory rates in pediatric (<8 years of age) population arefaster than respiratory rates in adults. In addition, the recommendeddepth of chest compression for pediatric victims (<8 years of age) is 1to 1.5 inches while the recommended chest compression depth for adultand pediatric (>8 years of age) is 1.5 to 2 inches.

Existing AEDs are unable to provide appropriate rescue protocol and ECGanalysis for a pediatric (<8 years of age) victim that is different froman adult rescue protocol and ECG analysis. Also, a lay rescuer who istrained on pediatric resuscitation and is not aware of the AHAguidelines recommendations will not be able to provide an effectiveresuscitation for a pediatric victim when using these existing AEDs.

SUMMARY

In a first aspect, the invention features a device for assisting arescuer in delivering therapy to an adult or pediatric patient, thedevice comprising a user interface comprising a display and/or audiospeakers, the user interface being configured to deliver prompts to arescuer to assist the rescuer in delivering therapy to a patient, aprocessor configured to provide prompts to the user interface and toperform an ECG analysis algorithm on ECG information detected from thepatient, at least one detection element configured to determine withoutrescuer input via the user interface that a pediatric patient is beingtreated, wherein if a pediatric patient is detected, the processormodifies the ECG analysis algorithm to use an ECG analysis algorithmconfigured for a pediatric patient rather than for an adult patient.

In a second aspect, the invention features a device for assisting arescuer in delivering therapy to an adult or pediatric patient, thedevice comprising a user interface comprising a display and/or audiospeakers, the user interface being configured to deliver prompts to arescuer to assist the rescuer in delivering therapy to a patient, aprocessor configured to provide prompts to the user interface and toperform an ECG analysis algorithm on ECG information detected from thepatient, at least one detection element configured to determine withoutrescuer input via the user interface that a pediatric patient is beingtreated, wherein if a pediatric patient is detected, the processormodifies the prompts provided to the user interface to use promptsadapted for a pediatric patient rather than for an adult patient.

In a third aspect, the invention features a device for assisting arescuer in delivering therapy to an adult or pediatric patient, thedevice comprising a user interface comprising a display and/or audiospeakers, the user interface being configured to deliver prompts to arescuer to assist the rescuer in delivering therapy to a patient, aprocessor configured to provide prompts to the user interface and toperform an ECG analysis algorithm on ECG information detected from thepatient, at least one detection element configured to determine withoutrescuer input via the user interface that a pediatric patient is beingtreated, wherein if a pediatric patient is detected, the processormodifies the CPR protocol that governs CPR prompts provided to the userinterface to use CPR prompts adapted for a pediatric patient rather thanfor an adult patient.

In preferred implementations, one or more of the following features maybe incorporated. The invention may further comprise an automaticexternal defibrillator for delivering defibrillation shocks to thepatient using defibrillation electrodes applied to the patient. Theprompts provided via the user interface may comprise prompts as to CPRchest compression, and the CPR chest compression prompts may be changedfrom an adult set of prompts to a pediatric set of prompts if apediatric patient is detected. The pediatric set of prompts may addressdepth and rate of CPR chest compressions. The invention may furthercomprise one or more sensors for measuring the rate and depth of CPRrelated chest compressions. The detection element may comprise circuitryfor detecting whether a pediatric or an adult defibrillation electrodeis in use. The detection element may comprise a force or pressure sensorlocated on a shoulder support element for sensing force or pressure fromthe weight of the patient. The energy of defibrillation shocks may bedetermined based in part on information as to the patient's weightobtained from the force or pressure sensor on the shoulder support. Theshoulder support element may comprise a removable cover of the device.The detection element may comprise one or more sensors for determiningfrom the separation of defibrillation electrodes placed on the patientwhether the patient is a pediatric or adult patient.

In a fourth aspect, the invention features an external defibrillationdevice for assisting a rescuer in delivering defibrillation therapy toan adult or pediatric patient, the device comprising a user interfacecomprising a display or audio speakers, the user interface beingconfigured to deliver prompts to a rescuer to assist the rescuer indelivering therapy to a patient, a processor configured to provideprompts to the user interface and to perform an ECG analysis algorithmon ECG information detected from the patient, a force or pressure sensorfor detecting information pertaining to the weight of the patient,wherein the processor modifies the defibrillation energy delivered tothe patient based on the information pertaining to the weight of thepatient.

In preferred implementations, one or more of the following features maybe incorporated. The processor may modify the ECG analysis algorithmbased on the information pertaining to the weight of the patient. Theforce or pressure sensor may be incorporated into a shoulder supportthat is placed under the shoulders of the patient. The shoulder supportmay be a cover for the defibrillator. The cover may have an uppersurface that is inclined at an angle that makes it suitable to be usedto properly position the patient's airway by lifting the patient'sshoulders to cause the patient's head to tilt back at an angle. Thecover may be configured to be positioned under a patient's neck andshoulders to support the patient's shoulders and neck in a way thathelps to maintain the patient's airway in an open position. Theinformation from sensors in the shoulder support element may becommunicated to the defibrillator by one or more of the followingtechniques: by a wire extending from the support to the defibrillator,or by a wireless communication connection between the support and thedefibrillator.

In a fifth aspect, the invention features an external defibrillationdevice for assisting a rescuer in delivering defibrillation therapy toan adult or pediatric patient, the device comprising a user interfacecomprising a display or audio speakers, the user interface beingconfigured to deliver prompts to a rescuer to assist the rescuer indelivering therapy to a patient, a processor configured to provideprompts to the user interface and to perform an ECG analysis algorithmon ECG information detected from the patient, a shoulder support elementfor placement under the shoulders of the patient to assist in keepingthe airway open, sensors in the shoulder support element for determiningif the patient's shoulders have been properly positioned on the element.

In preferred implementations, one or more of the following features maybe incorporated. The shoulder support element may comprise a cover forthe device.

In a sixth aspect, the invention features an external defibrillationdevice for assisting a rescuer in delivering defibrillation therapy toan adult or pediatric patient, the device comprising a user interfacecomprising a display or audio speakers, the user interface beingconfigured to deliver prompts to a rescuer to assist the rescuer indelivering therapy to a patient, a processor configured to provideprompts to the user interface and to perform an ECG analysis algorithmon ECG information detected from the patient, defibrillation electrodesfor placement on the chest of the patient, one or more sensors locatedin one or both of the defibrillation electrodes, the sensors beingconfigured to determine a distance between the electrodes after they areplaced on the patient's chest, wherein the processor can determineinformation pertaining to the size of the patient from the distancedetermined from the one or more sensors, and wherein the processor canvary the prompts, or the ECG analysis algorithm, or the energy deliveredto the patient based on the information pertaining to the size of thepatient.

In preferred implementations, one or more of the following features maybe incorporated. The processor may estimate the circumferential girth ofthe patient from the information obtained from the sensors. Theprocessor may estimate the age of the patient from the informationobtained from the sensors. Modifications to the ECG analysis algorithmmay include one or more of the following: heart rate criteria, QRS widthcriteria, VF frequency content criteria, or ECG amplitude criteria.Modifications to the prompts may include changing a sequence of prompts,a number of prompts, or a type of prompts. The prompts may includeprompts on CPR compression and CPR ventilation, and thecompression-ventilation ratio may be about 5:1 for pediatric patientsand about 15:2 for adult patients. The prompts may include prompts onCPR compression depth, and the desired compression depth for pediatricpatients may be in the range of about 1.0 to 1.5 inches, and the desiredcompression depth for adult patients may be in the range of about 1.0 to2.0 inches. The prompts may include a prompt informing the rescuer as towhether the device is operating in an adult or pediatric mode. Theprompts may include prompting of the CPR interval T1 based on one ormore of patient rhythm, age, or weight. The invention may furthercomprise one or more sensors and prompts for detecting and prompting theuser to achieve a complete chest release during CPR. The prompts mayinclude pediatric specific prompts for the compression rate R1. Theprompts may include adult specific prompts for the compression rate R1.

The invention may feature a system that will alter the AED arrhythmiaprocessing for adults or children based the automatic sensing or manualassignment of the patient type. Altering the AED arrhythmia processingfor pediatric subjects based on the pediatric specific logic may achievehigher sensitivity and specificity of the shock decision that willsignificantly improve the safety and effective of the device.

The invention may provide an improved method for providing anappropriate rescue protocol and ECG analysis based on patient age,thoracic circumferential girth and weight in an automated fashionwithout the need for any user intervention. Utilizing a means ofdetecting a patient's age, weight or thoracic circumferential girth, theAED can automatically switch to providing the appropriate rescueprotocol and optimizing performance of the ECG analysis algorithm for aspecific victim age and weight. If an untrained rescuer activates theproposed AED, the protocol is tailored to instruct the user to provideone minute of CPR to the pediatric (<8 years of age) victim beforeactivating the EMS system. The protocol is tailored to instruct the userto activate the EMS system before providing any treatment or CPR to anadult victim. Also, since the AED is capable of detecting the depth ofchest compression when used with a set of defibrillation electrodesembedding a chest compression detector, it can guide the rescuer toadminister appropriate chest compression-ventilation ratio and depth ofcompressions based on specific victim age and weight. Furthermore, theproposed AED can select a preconfigured CPR period length based on thetype of rhythm when the CPR interval is entered. For example, thepre-programmed CPR period when an asystole, PEA, or normal rhythm isdetected can be longer than after a ventricular fibrillation ortachycardia is detected.

The invention may provide a more comprehensive and effective system fordelivering treatment to pediatric arrest victims, providing anappropriate rescue protocol and ECG analysis based on patient age,thoracic circumferential girth and weight in an automated fashionwithout the need for any user intervention.

The invention may feature a device for assisting a rescuer in deliveringtherapy to an adult or pediatric patient, the device comprising a userinterface comprising a display or audio speakers, the user interfacebeing configured to deliver prompts to a rescuer to assist the rescuerin delivering therapy to a patient; a processor configured to provideprompts to the user interface and to perform an ECG analysis algorithmon ECG information detected from the patient; at least one detectionelement configured to determine without rescuer input via the userinterface that a pediatric patient is being treated; wherein, if apediatric patient is detected, the processor modifies the ECG analysisalgorithm or the prompts provided to the user interface to use an ECGanalysis algorithm or prompts better suited to a pediatric patient thanto an adult patient.

The device may incorporate an automatic external defibrillator fordelivering defibrillation shocks to the patient using defibrillationelectrodes applied to the patient. The prompts provided via the userinterface may comprise prompts as to CPR chest compression, and the CPRchest compression prompts are changed from an adult set of prompts to apediatric set of prompts if a pediatric patient is detected. Thepediatric set of prompts may address depth and rate of CPR chestcompressions. One or more sensors for measuring the rate and depth ofCPR related chest compressions may be provided. The detection elementmay comprise circuitry for detecting whether a pediatric or an adultdefibrillation electrode is in use. The detection element may comprise aforce or pressure sensor located on a shoulder support element forsensing force or pressure from the weight of the patient. The energy ofdefibrillation shocks may be determined based in part on information asto the patient's weight obtained from the force or pressure sensor onthe shoulder support. The shoulder support element may comprise aremovable cover of the device. The detection element may comprise one ormore sensors for determining from the separation of defibrillationelectrodes placed on the patient whether the patient is a pediatric oradult patient.

The AED may include the capability of measuring the rate and depth ofCPR related chest compressions and automatically switch when specificdefibrillation electrode types are detected to provide appropriaterescue protocol, ECG analysis, and CPR interval length and guidancebased on the victim's determined age. Based on the determined patientage, appropriate ventilation to compression ratio and compressioninterval length are determined, and guidance is provided to the rescuerto provide appropriate chest compressions/ventilation ratio and rate andcompression depth via voice and text prompts throughout the entirerescue process.

The invention may feature an external defibrillation device forassisting a rescuer in delivering defibrillation therapy to an adult orpediatric patient. The device may comprise a user interface comprising adisplay or audio speakers, the user interface being configured todeliver prompts to a rescuer to assist the rescuer in delivering therapyto a patient; a processor configured to provide prompts to the userinterface and to perform an ECG analysis algorithm on ECG informationdetected from the patient; a force or pressure sensor for detectinginformation pertaining to the weight of the patient; wherein theprocessor modifies the defibrillation energy delivered to the patientbased on the information pertaining to the weight of the patient.

The processor may modify the ECG analysis algorithm based on theinformation pertaining to the weight of the patient. The force orpressure sensor may be incorporated into a shoulder support that isplaced under the shoulders of the patient. The shoulder support may be acover for the defibrillator. The cover may have an upper surface that isinclined at an angle that makes it suitable to be used to properlyposition the patient's airway by lifting the patient's shoulders tocause the patient's head to tilt back at an angle. The cover may beconfigured to be positioned under a patient's neck and shoulders tosupport the patient's shoulders and neck in a way that helps to maintainthe patient's airway in an open position. The information from sensorsin the shoulder support element may be communicated to the defibrillatorby one or more of the following techniques: by a wire extending from thesupport to the defibrillator, or by a wireless communication connectionbetween the support and the defibrillator.

Some implementations may provide an automated means for determining theage of the victim with greater specificity. Victim weight is a commonlyused clinical measure for determining defibrillation energies forchildren. An integrated force sensor may be provided within the AED formeasuring the patient's weight and the AED will then adjust thedefibrillation energy and ECG analysis parameters based on the measuredweight.

The force sensor may be incorporated into the cover of the AED. Thecover has an upper surface that is inclined at an angle that makes itsuitable to be used to properly position the patient's airway, by, forinstance, lifting the patient's shoulders thereby causing the patient'shead to tilt back at the proper angle. The cover is constructed to bepositioned under a patient's neck and shoulders to support the patient'sshoulders and neck in a way that helps to maintain his airway in an openposition, i.e., maintaining the patient in the head tuck-chin liftposition. When a caregiver encounters a person who appears to besuffering from cardiac arrest, the caregiver should follow recommendedresuscitation procedures, such as are specified by the AHA Guidelinesfor Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Ifthere is no evidence of head or neck trauma, the caregiver should clearany debris from the patient's airway. After this has been done, thecaregiver should roll the patient onto his side, place cover under thepatient's shoulders, and roll the patient back onto his back. The covershould be positioned so as to support the patient in the head tilt-chinlift position. The caregiver can then proceed with CPR and/or use of thedefibrillator. The positions (a patient in the head lift-chin tiltposition and a patient with a closed airway) are also shown in the AHAGuidelines for Cardiopulmonary Resuscitation and EmergencyCardiovascular Care, Aug. 22, 2000, p. I-32, FIGS. 7 and 8. The cover isprovided with a detection means for determining if the patient'sshoulders have been properly positioned on the cover. Communication ofthe detection means located in the cover to the processor in the devicehousing can be accomplished by making the cover an integral element ofthe device housing, for instance via a hinge element or by providing aninterconnection element such as a flat flexible cable. Communication mayalso be accomplished wirelessly via such technologies as Bluetooth orinductive methods. When the patient's shoulders are placed on the cover,the measured force is communicated to the AED.

The invention may feature an external defibrillation device forassisting a rescuer in delivering defibrillation therapy to an adult orpediatric patient, the device comprising a user interface comprising adisplay or audio speakers, the user interface being configured todeliver prompts to a rescuer to assist the rescuer in delivering therapyto a patient; a processor configured to provide prompts to the userinterface and to perform an ECG analysis algorithm on ECG informationdetected from the patient; a shoulder support element for placementunder the shoulders of the patient to assist in keeping the airway open;sensors in the shoulder support element for determining if the patient'sshoulders have been properly positioned on the element.

The invention may feature an external defibrillation device forassisting a rescuer in delivering defibrillation therapy to an adult orpediatric patient, the device comprising a user interface comprising adisplay or audio speakers, the user interface being configured todeliver prompts to a rescuer to assist the rescuer in delivering therapyto a patient; a processor configured to provide prompts to the userinterface and to perform an ECG analysis algorithm on ECG informationdetected from the patient; defibrillation electrodes for placement onthe chest of the patient; one or more sensors located in one or both ofthe defibrillation electrodes, the sensors being configured to determinea distance between the electrodes after they are placed on the patient'schest; wherein the processor can determine information pertaining to thesize of the patient from the distance determined from the one or moresensors, and wherein the processor can vary the prompts, or the ECGanalysis algorithm, or the energy delivered to the patient based on theinformation pertaining to the size of the patient.

The processor may estimate the circumferential girth of the patient fromthe information obtained from the sensors. The processor may estimatethe age of the patient from the information obtained from the sensors.

The sensor elements may be fabricated into the two defibrillationelectrodes placed on the victim's chest. The electrodes may beconstructed such that the relative distance between the electrodes canbe determined by the AED. Based on that relative distance, thecircumferential girth can be calculated by the AED and used as a meansof estimating patient age as well as delivering the appropriate energylevel.

Other features and advantages of the invention will be apparent from thedescription and drawings, and from the claims.

DESCRIPTION OF DRAWINGS

FIG. 1 is a perspective view of an AED with its cover on.

FIG. 2 is a perspective view of the AED of FIG. 1 with the coverremoved.

FIG. 3 is a block diagram of the AED.

FIG. 4 is a plan view of the graphical interface decal used on the coverof the AED of FIG. 1.

FIG. 5 is a plan view of the graphical interface decal used on thedevice housing of the AED of FIG. 1, as shown in FIG. 2.

FIG. 6 a is a flow diagram for the pediatric AED resuscitation protocol.

FIG. 6 b is a flow diagram for the adult AED resuscitation protocol.

FIG. 7 shows an exploded perspective view of the cover and housing.

FIG. 8 shows a side plan view of the cover indicating angle ‘A’.

FIGS. 9 a and 9 b show the effect on the patient's airway of placing thecover beneath a patient's shoulders.

FIG. 10 shows the graphical instructions on the cover for placing thecover under a patient's shoulders.

FIG. 11 shows an integrated electrode pad.

FIG. 12 is a flow diagram of the arrhythmia processing in the AED.

FIG. 13 is a flow diagram of mode specific processing for enhancing QRSdetection.

FIG. 14 is a flow diagram of mode specific processing for enhancingrhythm classification logic and shock determination.

FIG. 15 is an example AED arrhythmia logic table for an adult.

FIG. 16 is an example AED arrhythmia logic table for a child.

DETAILED DESCRIPTION

There are a great many possible implementations of the invention, toomany to describe herein. Some possible implementations that arepresently preferred are described below. It cannot be emphasized toostrongly, however, that these are descriptions of implementations of theinvention, and not descriptions of the invention, which is not limitedto the detailed implementations described in this section but isdescribed in broader terms in the claims.

The terms “caregiver”, “rescuer” and “user” are used interchangeably inthe description of the invention and refer to the operator of the deviceproviding care to the patient. “Victim” is also used interchangeablywith “patient”.

Referring to FIGS. 1 and 2, an automated external defibrillator 10includes a removable cover 12 and a device housing 14. The defibrillator10 is shown with cover 12 removed in FIG. 2. An electrode assembly 16(or a pair of separate electrodes) is connected to the device housing 14by a cable 18. Electrode assembly 16 is stored under cover 12 when thedefibrillator is not in use.

Referring to FIG. 3, the invention includes a processor means 20, a userinterface 21 including such elements as a graphical 22 or text display23 or an audio output such as a speaker 24, and a detection means 25 fordetermining whether at least one of a series of steps in a protocol hasbeen completed successfully. In the preferred embodiment, the detectionmeans 25 also includes the ability to determine both whether aparticular step has been initiated by a user and additionally whetherthat particular step has been successfully completed by a user. Based onusability studies in either simulated or actual use, common user errorsare determined and specific detection means are provided for determiningif the most prevalent errors have occurred.

Device housing 14 includes a power button 15 and a status indicator 17.Status indicator 17 indicates to the caregiver whether the defibrillatoris ready to use.

The cover 12 includes a cover decal 30 (FIGS. 1 and 4) including a logo31 and a series of graphics 32, 34 and 36. Logo 31 may provideinformation concerning the manufacturer of the device and that thedevice is a defibrillator (e.g., “ZOLL AED”, as shown in FIG. 1,indicating that the device is a Semi-automatic External Defibrillatoravailable from ZOLL Medical). Graphics 32, 34 and 36 lead the caregiverthrough the initial stages of a cardiac resuscitation sequence asoutlined in the AHA's AED treatment algorithm for Emergency Cardiac Carepending arrival of emergency medical personnel. (See “Guidelines 2000for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Supplement to Circulation,” Volume 102, Number 8, Aug. 22, 2000, pp.I-67.) Thus, graphic 32, showing the caregiver and patient, indicatesthat the caregiver should first check the patient for responsiveness,e.g., by shaking the patient gently and asking if the patient is okay.Next, graphic 34, showing a telephone and an emergency vehicle,indicates that the caregiver should call for emergency assistance priorto administering resuscitation. Finally, graphic 36 indicates that afterthese steps have been performed the caregiver should remove the cover 12of the defibrillator, remove the electrode assembly 16 stored under thelid, and turn the power on by depressing button 15. The graphics arearranged in clockwise order, with the first step in the upper left,since this is the order most caregivers would intuitively follow.However, in this case the order in which the caregiver performs thesteps is not critical, and thus for simplicity no other indication ofthe order of steps is provided.

The cover 12 is constructed to be positioned under a patient's neck andshoulders, as shown in FIGS. 9 a and 9 b to support the patient'sshoulders and neck in a way that helps to maintain his airway in an openposition, i.e., maintaining the patient in the head tuck-chin liftposition. The cover is preferably formed of a relatively rigid plasticwith sufficient wall thickness to provide firm support duringresuscitation. Suitable plastics include, for example, ABS,polypropylene, and ABS/polypropylene blends.

Prior to administering treatment for cardiac arrest, the caregivershould make sure that the patient's airway is clear and unobstructed, toassure passage of air into the lungs. To prevent obstruction of theairway by the patient's tongue and epiglottis (e.g., as shown in FIG. 9a), it is desirable that the patient be put in a position in which theneck is supported in an elevated position with the head tilted back anddown. Positioning the patient in this manner is referred to in theAmerican Heart Association Guidelines for Cardiopulmonary Resuscitationand Emergency Cardiovascular Care as the “head tilt-chin lift maneuver.”The head tilt-chin lift position provides a relatively straight, openairway to the lungs through the mouth and trachea. However, it may bedifficult to maintain the patient in this position during emergencytreatment.

The cover 12 has an upper surface 24 that is inclined at an angle A(FIG. 8) of from about 10 to 25 degrees, e.g., 15 to 20 degrees, so asto lift the patient's shoulders and thereby cause the patient's head totilt back. The upper surface 24 is smoothly curved to facilitatepositioning of the patient. A curved surface, e.g., having a radius ofcurvature of from about 20 to 30 inches, generally provides betterpositioning than a flat surface. At its highest point, the cover 12 hasa height H (FIG. 8) of from about 7.5 to 10 cm. To accommodate the widthof most patients' shoulders, the cover 12 preferably has a width W (FIG.8) of at least 6 inches, e.g., from about 6 to 10 inches. If the cover12 is not wide enough, the patient's neck and shoulders may move aroundduring chest compressions, reducing the effectiveness of the device. Thepositions shown in FIGS. 9 a and 9 b (a patient in the head lift-chintilt position and a patient with a closed airway) are also shown in theAHA Guidelines for Cardiopulmonary Resuscitation and EmergencyCardiovascular Care, Aug. 22, 2000, p. I-32, FIGS. 7 and 8.

In a preferred implementation, if on power-up, the AED detects that thepediatric defibrillation pads are attached then the AED willautomatically start a pediatric rescue protocol. FIG. 6 a shows thedetails of one instance of the pediatric protocol. The device willoutput voice/text prompts indicating to the rescuer to check thevictim's responsiveness (i.e., “Check Responsiveness”) and allow apreprogrammed time interval (e.g., 4 seconds) to allow for checking theresponsiveness before moving to the next state. The device will nextoutput voice/text prompts instructing the rescuer to check breathing(example “Check Breathing”) and then allow a preprogrammed time interval(e.g., 7 seconds) to check the victim's breathing. The AED will nextoutput voice/text prompts instructing the rescuer to check the victim'spulse (example “Check Pulse”) and then allow a preprogrammed timeinterval (e.g., 10 sec) for checking the victim's pulse. The AED willthen enter a CPR state where it outputs voice/text prompts instructingthe rescuer to start chest compressions (e.g., “If No Pulse, Start ChestCompressions”). While in this CPR state, the chest compression signal isreceived by ‘Detect & Increment Chest Compressions Counter’ functionthat detects chest compressions and counts them. While the number ofchest compressions is less than 5, the depth of each detectedcompression is evaluated. If the depth of the detected compression isnot higher than 1″, the rescuer is instructed to push harder on thevictims chest by outputting “Push Harder” voice/text prompts and returnto ‘Detect & Increment Chest Compression count’ state. Else, if thedepth of the detected chest compression exceeds 1″, this depth isevaluated again. If the depth of the detected compression is less than1.5″, a check is made for complete hand release to allow the victim'schest to recoil. If the rescuer hand is released off the victim chestafter every compression, then the AED checks if the compression rate ishigher than a preprogrammed R1 rate. If the compression rate is higherthan R1, the AED output voice/text prompts indicating effectivecompressions “Good Compressions”. Else, the compression rate is lessthan R1, the AED output voice/text prompts instructing the rescuer topress faster and return to ‘Detect & Increment Chest Compression count’state.

If the rescuer is not releasing the hands off the chest after eachcompression, the AED instructs the user to release the hands off thevictim's chest after each compression by outputting voice/text prompts“Release Hands Off Chest After Pushing”, then returns to ‘Detect &Increment Chest Compressions Count’ state. If the depth of the detectedchest compression is greater than 1.5″, the AED instructs the rescuer topush on the victim chest with less force by outputting the prompt “PushWith Less Force”, then returns to ‘Detect & Increment Chest CompressionsCount’ state. If the number of chest compressions exceeds 5, the deviceinstructs the rescuer to stop compressions and give the victim onebreath by outputting voice/text prompts “Stop Compressions, Give OneBreath”, then checks if the CPR state time interval exceeds a timer T1.If CPR state time interval is less than T1, the chest compressioncounter is reset and the AED returns to ‘Detect & Increment ChestCompressions Count’ state. If the CPR state time interval exceeds T1,the AED instructs the rescuer to activate the EMS system by calling 911and then the AED transitions to ‘Execute 3Shock Sequence, Set T1’ state.In this state, the “Pediatric ECG Analysis Algorithm” is executed. Ifthe first analysis detects a non-shockable rhythm, the AED transitionsto the CPR state for another cycle of CPR. Else, if the first analysisdetects a shockable rhythm, the rescuer is advised to deliver adefibrillation shock. Following the shock delivery a second analysis isautomatically initiated to determine whether the defibrillationtreatment was successfull or not (i.e. the shockable ECG rhythm has beenconverted to a normal or other non-shockable rhythm). If this secondanalysis detects the continuing presence of a shockable arrhythmia, theAED advises the user to deliver a second defibrillation treatment.

A third ECG analysis is automatically initiated to determine whether thesecond shock was or was not effective. If a shockable rhythm persists,the rescuer is then advised to deliver a third defibrillation treatment.Following the third defibrillator shock or when any of the analysesdescribed above detects a non-shockable rhythm, the AED transitions tothe CPR state for another cycle of chest compressions and ventilation.Also In the ‘Execute 3 Shock Sequence, Set T1’ state, T1 is set to apreprogrammed value based on the type of the detected rhythm: normal,asystole, non-conductive, ventricular tachycardia or ventricularfibrillation. For instance, the asystole and non-conductive rhythms mayrequire longer CPR periods than 1 minute in such case the ‘Execute 3Shock Sequence, Set T1’ task will set the T1 to a preprogrammed valueappropriate for pediatric asystole or non-conductive rhythms that may belonger than one minute. In the case of an arrhythmia, the required CPRtime may be only 1 minute in such case the ‘Execute 3 Shock Sequence,Set T1’ task will set the T1 to a preprogrammed value appropriate forpediatric arrhythmia rhythms that may be one minute. In the case ofnormal rhythm, the required CPR time may be only 1 minute in such casethe ‘Execute 3 Shock Sequence, Set T1’ task will set the T1 to apreprogrammed value appropriate for pediatric pediatric rhythms that maybe one minute or longer.

If on the other hand, the AED detects adult defibrillation pads onpower-up, the AED will automatically start an adult rescue protocol.FIG. 6 b shows the details of one instance of the adult rescue protocol.The AED will output voice/text prompts indicating to the rescuer tocheck the victim's responsiveness (i.e., “Check Responsiveness”) andallow a preprogrammed time interval (i.e., 4 seconds) to expire to allowfor checking the responsiveness before moving to the next state. Next,the AED instructs the rescuer to activate the EMS system by calling 911and allow a preprogrammed time interval (e.g., 4 seconds) to expire toallow someone call for help before moving to the next state. The AEDwill next output voice/text prompts instructing the rescuer to checkbreathing (e.g., “Check Breathing”) and then allow a preprogrammed timeinterval (example: 7 seconds) to check breathing. The device will nextoutput voice/text prompts instructing the rescuer to check the victim'spulse (e.g., “Check Pulse”) and then allow a preprogrammed time interval(e.g., 10 seconds) for the pulse check. The AED will then transitions to‘Execute 3 Shock Sequence, Set T1’ state. In this state, the “Adult ECGAnalysis Algorithm” is executed. If the first analysis detects anon-shockable rhythm, the AED will transition to the CPR state. Else, ifthe first analysis detects a shockable rhythm, the rescuer is advised todeliver a defibrillation shock.

Following the shock delivery a second analysis is automaticallyinitiated to determine whether the defibrillation treatment wassuccessful or not (i.e. the shockable ECG rhythm has been converted to anormal or other non-shockable rhythm). If this second analysis detectsthe continuing presence of a shockable arrhythmia, the AED advises theuser to deliver a second defibrillation treatment. A third ECG analysisis automatically initiated to determine whether the second shock was orwas not effective. If a shockable rhythm persists, the rescuer is thenadvised to deliver a third defibrillation treatment. Following the thirddefibrillator shock or when any of the analyses described above detectsa non-shockable rhythm, the device transition to the CPR state foranother cycle of CPR. Also In the ‘Execute 3 Shock Sequence, Set T1state, T1 is set to a preprogrammed value based on the type of thedetected rhythm: normal, asystole, non-conductive, ventriculartachycardia or ventricular fibrillation. For instance, the asystole andnon-conductive rhythms may require longer CPR periods than 1 minute insuch case the ‘Execute 3 Shock Sequence, Set T1’ task will set the T1 toa preprogrammed value appropriate for adult asystole or non-conductiverhythms that may be longer than one minute. In the case of anarrhythmia, the required CPR time may be only 1 minute in such case the‘Execute 3 Shock Sequence, Set T1 task will set the T1 to apreprogrammed value appropriate for adult arrhythmia rhythms that may beone minute. In the case of normal rhythm, the required CPR time may beonly 1 minute in such case the ‘Execute 3 Shock Sequence, Set T1 taskwill set the T1 to a preprogrammed value appropriate for adult rhythmsthat may be one minute or longer. Upon entering the CPR state, the AEDoutputs voice/text prompts instructing the rescuer to start chestcompressions (example “If No Pulse, Start Chest Compressions”). While inthis CPR state the chest compression signal is received by ‘Detect &Increment Chest Compressions Counter’ function that detects chestcompressions and counts them. While the number of chest compressions isless than 15, the depth of each detected compression is evaluated. Ifthe depth of the detected compression is not higher than 1.5″, therescuer is instructed to push harder on the victims chest by outputting“Push Harder” voice/text prompts and return to ‘Detect & Increment ChestCompression count’ state. Else, if the depth of the detected chestcompression exceeds 1.5″, this depth is evaluated again. If the depth ofthe detected compression is less than 2″, a check is made for completehand release. If the rescuer hand is released off the victim chest afterevery compression to allow for complete chest recoil, then the AEDchecks if the compression rate is higher than a preprogrammed R1 rate.If the compression rate is higher than R1, the AED output voice/textprompts indicating effective compressions “Good Compressions”. Else, thecompression rate is less than R1, the AED output voice/text promptsinstructing the rescuer to press faster and return to ‘Detect &Increment Chest Compression count’ state.

If the rescuer is not releasing the hands off the chest after eachcompression, the device instructs the user to release the hands off thevictim's chest after each compression to provide more effective CPR byoutputting voice/text prompts “Release Hands Off Chest After Pushing”,then returns to ‘Detect & Increment Chest Compressions Count’ state. Ifthe depth of the detected chest compression is greater than 3″, thedevice instructs the rescuer to push on the victim chest with less forceby outputting the prompt “Push With Less Force”, then checks ifcompression rate is higher than a preprogrammed R1 rate. If thecompression rate is higher than R1, the AED output voice/text promptsindicating effective compressions. Else, the compression rate is lessthan R1, the AED output voice/text prompts instructing the rescuer topress faster. If the number of chest compressions exceeds 15, the deviceinstructs the rescuer to stop compressions and give the victim twobreaths by outputting voice/text prompts “Stop Compressions, Give TwoBreaths”, then checks if the CPR state time interval exceeds a selectedtimer T1.

If CPR state time interval is less than T1, the chest compressioncounter is reset and the device returns to ‘Detect & Increment ChestCompressions Count’ state. If the CPR state time interval exceeds T1,the AED will transition to ‘Execute 3 Shock Sequence, Set T1 state.

FIG. 12 shows an example of a AED Arrhythmia processing flow diagram.Since the pediatric QRS is narrower and the heart faster than adult, theQRS detection system can be tailored to be more sensitive to the ECGsignal. The flow diagram also shows that the arrhythmia classificationlogic and shock decision logic can be altered to improve the specificityand sensitivity.

In the Signal Conditioning block, the ECG signal is band passed andnotch filtered to remove baseline offsets, high frequency noise, andline noise frequency noise. The noise Detection block performs baseline,motion, high frequency, muscle, and saturation noise detections andflags the ECG Signal status data accordingly.

In the QRS detection block, the processing produces a QRS detectionsignal by performing a QRS based matched filter on the filtered ECGdata. The type of processing performed is dependant on the ProcessingMode Setting (reference FIG. 13).

Once the location of the QRS is detected in the signal stream, the QRSDetection Block will process the signal around the QRS detection todetermine specific measurements such as R-R interval, QRS width, QRSarea, and other features which will support classification of the QRScomplex and its underlying rhythm. The Rhythm Measurement block willperform analysis on the QRS measures and ECG signal to produce rhythmbased measures required for rhythm classification. The RhythmDetermination and Shock Determination Decision Logic block will processthe QRS detection and rhythm data to classify the ECG rhythm and make ashock versus no shock decision. Many beat and rhythm classificationtechniques are know in the art and include heuristic logic,morphological analysis, expert system analysis, and statisticalclustering techniques. The outputs from the Rhythm Determination andShock Determination Decision Logic block are used by the AED to shockthe victim (fully automatic AED) or notify the user to deliver a shock(semi-automatic AED) or begin other interventions such as CPR.

FIG. 13 shows an example of the use of mode specific processing toenhance QRS detection. In the PEDI Mode selection block, the matchedfilter characteristics are chosen based on the Processing Mode setting(Adult or Pediatric) to produce an optimal detection signal for thatclass of patients. A threshold detection scheme is used to determine thelocation of the QRS complexes in the detection signal. A thresholdsystem is utilized which has been optimized for use with the respectiveQRS matched filter. The QRS Detection Selection block determines whetherto perform QRS Measurements (QRS Detected) or perform an Asystole Check(QRS Not Detected). The Asystole check will process a detection timeout,adjust detection thresholds, and notify the target system if an asystolestate is present.

FIG. 14 shows an example of the use of mode specific processing toenhance the rhythm classification logic and shock decisiondetermination. The PEDI Mode Selection block chooses which Patient ModeRhythm Logic to process. Rhythm classification logic can be implementedin a number of ways, heuristic (if-then-else) rules, feature clusteranalysis, fuzzy system analysis, neural networks, Bayesian probabilisticsystem analysis, etc. The Shockable Rhythm Selection block selects theappropriate process flow based on the Shock decision. The No ShockDecision block notifies the defibrillator system to take the appropriateactions such as display and audibly announce the non-shockable rhythmanalysis result. A shockable decision will produce a charging of thedefibrillator and a delivery of therapy (automatic defibrillator) or aprompt to the user for delivery of energy (semi-automaticdefibrillator).

FIG. 15 and FIG. 16 are simple examples adult and pediatric AEDarrhythmia logic tables. The rhythm classifications in column 1 aresatisfied when all of the rules stated in columns 2-6 are met and therespective shock decision is listed in the last column. The examplesshow that the shockable versus non-shockable decision can come fromspecific adult or pediatric rhythm classification logic. The variouslimits, rules, or other population specific logic systems are tuned (ortrained) from adult and pediatric ECG signal databases, respectively.

Referring to FIG. 7, the cover 12 is provided with a detection means fordetermining if the patient's shoulders have been properly positioned onthe cover 12. Two photoelectric sensors 156, 157 are used to determineif the cover has been placed underneath the patient's back. The sensors156, 157 are located along the acute edge of the cover 12, with onefacing inward and one facing outward with the cable 155 providing bothpower to the sensors 156, 157 as well as detection of the sensor output.If the cover 12 is upside down, the inner sensor 156 will measure ahigher light level than the outer sensor 157; if the cover has beenplaced with the acute edge facing toward the top of the patient's head,then the outer sensor 157 will measure higher than the inner sensor 156and will also exceed a pre-specified level. In the case of a properlypositioned cover, both inner 156 and outer sensor 157 outputs will bebelow a pre-specified level. In another embodiment, the detections meansis provided by a pressure sensor 158 located underneath the cover decal.The pressure sensor 158 can be used to measure the thoracic weight ofthe victim. Based on the measured weight, a table lookup can begenerated, determining the victim's approximate age as well as theoptimal defibrillation energies to provide.

Thus, when a person collapses and a caregiver suspects that the personis in cardiac arrest, the caregiver first gets the defibrillator andturns the power on 102. If the unit passes its internal self tests, andis ready for use, this will be indicated by indicator 17. Next, thedefibrillator prompts the caregiver with an introductory audio message,e.g., “Stay calm. Listen carefully.”

Shortly thereafter, the defibrillator will prompt the caregiver with anaudio message indicating that the caregiver should check the patient forresponsiveness. Simultaneously, the LED 56 adjacent graphic 42 willlight up, directing the caregiver to look at this graphic. Graphic 42will indicate to the caregiver that she should shout “are you OK?” andshake the person in order to determine whether the patient isunconscious or not.

After a suitable period of time has elapsed (e.g., 2 seconds), if thecaregiver has not turned the defibrillator power off (as would occur ifthe patient were responsive), the defibrillator will give an audioprompt indicating that the caregiver should call for help.Simultaneously, the LED adjacent graphic 42 will turn off and the LEDadjacent graphic 43 will light up, directing the caregiver's attentionto graphic 43. Graphic 43 will remind the caregiver to call emergencypersonnel, if the caregiver has not already done so.

After a suitable interval has been allowed for the caregiver to performthe prior step (e.g., 2 seconds) the defibrillator will give an audioprompt indicating that the caregiver should open the patient's airwayand check whether the patient is breathing. The LED adjacent graphic 43will turn off, and the LED adjacent graphic 44 will light up, directingthe caregiver's attention to graphic 44, which shows the properprocedure for opening a patient's airway. This will lead the caregiverto lift the patient's chin and tilt the patient's head back. Thecaregiver may also position an airway support device under the patient'sneck and shoulders, if desired, as discussed below with reference toFIGS. 9 a, 9 b. The caregiver will then check to determine whether thepatient is breathing.

After a suitable interval (e.g., 15 seconds), the defibrillator willgive an audio prompt indicating that the caregiver should check forsigns of circulation, the LED adjacent graphic 44 will turn off, and theLED adjacent graphic 45 will light up. Graphic 45 will indicate to thecaregiver that the patient should be checked for a pulse or other signsof circulation as recommended by the AHA for lay rescuers.

After a suitable interval (e.g., 5 to 7 seconds), the defibrillator willgive an audio prompt indicating that the caregiver should attachelectrode assembly 16 to the patient, the LED adjacent graphic 45 willturn off, and the LED adjacent graphic 46 will light up. Graphic 46 willindicate to the caregiver how the electrode assembly 16 should bepositioned on the patient's chest.

At this point, the LED adjacent graphic 47 will light up, and thedefibrillator will give an audio prompt indicating that the patient'sheart rhythm is being analyzed by the defibrillator and the caregivershould stand clear. While this LED is lit, the defibrillator willacquire ECG data from the electrode assembly, and analyze the data todetermine whether the patient's heart rhythm is shockable. This analysisis conventionally performed by AEDs.

If the defibrillator determines that the patient's heart rhythm is notshockable, the defibrillator will give an audio prompt such as “No shockadvised”. The LEDs next to graphics 48 and 49 will then light up, andthe defibrillator will give an audio prompt indicating that thecaregiver should again open the patient's airway, check for breathingand a pulse, and, if no pulse is detected by the caregiver, thencommence giving CPR. Graphics 48 and 49 will remind the caregiver of theappropriate steps to perform when giving CPR.

Alternatively, if the defibrillator determines that the patient's heartrhythm is shockable, the defibrillator will give an audio prompt such as“Shock advised. Stand clear of patient. Press treatment button.” At thesame time, the heart 54 and/or hand 52 will light up, indicating to thecaregiver the location of the treatment button. At this point, thecaregiver will stand clear (and warn others, if present, to stand clear)and will press the heart 54, depressing the treatment button andadministering a defibrillating shock (or a series of shocks, asdetermined by the defibrillator electronics) to the patient.

Referring to FIG. 11, in some implementations, a means is provided ofdetecting the relative lateral positions of the apex electrode 255 andthe sternum electrode 254. In one implementation, magnetic Hall Effectsensors 251 are located such that when activated by the magnet 253located within the apex electrode 255 the signal generated by the Halleffect sensor 251 indicates the relative lateral location of theelectrodes. Using known anthropometrics, the thoracic girth can beestimated as well as patient age and defibrillation energy levels. Therelative lateral positions of the electrodes can be determined using alinear encoder commonly used in digital calipers thus providing anaccurate measurement of girth. The encoder may be an optical encoder ora magnetic based encoder.

The cover 12 of the AED may include a decal on its underside, e.g.,decal 200 shown in FIG. 10. Decal 200 illustrates the use of the coveras a passive airway support device, to keep the patient's airway openduring resuscitation. Graphic 202 prompts the caregiver to roll thepatient over and place cover 12 under the patient's shoulders, andgraphic 204 illustrates the proper positioning of the cover 12 under thepatient to ensure an open airway.

While such a graphic is not included in the decal shown in FIG. 5, thedecal 40 may include a graphic that would prompt the user to check tosee if the patient is breathing. Such a graphic may include, e.g., apicture of the caregiver with his ear next to the patient's mouth. Thegraphic may also include lines indicating flow of air from the patient'smouth.

Many other implementations of the invention other than those describedabove are within the invention, which is defined by the followingclaims.

What is claimed is:
 1. A device for assisting a rescuer in deliveringtherapy to an adult or pediatric patient, the device comprising a userinterface comprising a display and/or audio speakers, the user interfacebeing configured to deliver prompts to a rescuer to assist the rescuerin delivering therapy to a patient; a processor configured to provideprompts to the user interface and to perform an ECG analysis algorithmon ECG information detected from the patient; at least one detectionelement configured to make a determination without rescuer input via theuser interface that a pediatric patient is being treated, wherein thedetection element is configured to make the determination based on theoutput of a force or pressure sensor for sensing force or pressure fromthe weight of the patient; wherein if the determination is that apediatric patient is being treated, the processor modifies the ECGanalysis algorithm to use an ECG analysis algorithm configured for apediatric patient rather than for an adult patient.
 2. The device ofclaim 1 further comprising an automatic external defibrillator fordelivering defibrillation shocks to the patient using defibrillationelectrodes applied to the patient.
 3. The device of claim 2 wherein thedetection element comprises circuitry for detecting whether a pediatricor an adult defibrillation electrode is in use.
 4. The device of claim 2wherein the force or pressure sensor is located on a shoulder supportelement.
 5. The device of claim 4 wherein the shoulder support elementcomprises a removable cover of the device.
 6. The device of claim 1wherein the energy of defibrillation shocks is determined based in parton information as to the patient's weight obtained from the force orpressure sensor.
 7. The device of claim 1 wherein modifications to theECG analysis algorithm include one or more of the following: heart ratecriteria, QRS width criteria, VF frequency content criteria, or ECGamplitude criteria.
 8. The device of claim 1 wherein the processorfurther modifies prompts, including changing a sequence of prompts, anumber of prompts, or a type of prompts.
 9. The device of claim 1wherein the processor further modifies prompts, and wherein the promptsinclude prompts on CPR compression and CPR ventilation, and thecompression-ventilation ratio is about 5:1 for pediatric patients andabout 15:2 for adult patients.
 10. The device of claim 1 wherein theprocessor further modifies prompts, and wherein the prompts includeprompts on CPR compression depth, and the desired compression depth forpediatric patients is in the range of about 1.0 to 1.5 inches, and thedesired compression depth for adult patients is in the range of about1.0 to 2.0 inches.
 11. The device of claim 1 wherein the processorfurther modifies prompts, and wherein the prompts include a promptinforming the rescuer as to whether the device is operating in an adultor pediatric mode.
 12. The device of claim 1 wherein the processorfurther modifies prompts, and wherein the prompts include prompting ofthe CPR interval T1 based on one or more of patient rhythm, age, orweight.
 13. The device of claim 1 wherein the processor further modifiesprompts, and further comprising one or more sensors and prompts fordetecting and prompting the user to achieve a complete chest releaseduring CPR.
 14. The device of claim 1 wherein the processor furthermodifies prompts, and wherein the prompts include pediatric specificprompts for the compression rate R1.
 15. The device of claim 1 whereinthe processor further modifies prompts, and wherein the prompts includeadult specific prompts for the compression rate R1.
 16. The device ofclaim 4 wherein the information from sensors in the shoulder supportelement is communicated to the defibrillator by one or more of thefollowing techniques: by a wire extending from the support to thedefibrillator, or by a wireless communication connection between thesupport and the defibrillator.